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2KLL

Solution structure of human interleukin-33

Summary for 2KLL
Entry DOI10.2210/pdb2kll/pdb
NMR InformationBMRB: 16317
DescriptorInterleukin-33 (1 entity in total)
Functional Keywordsinterleukin, beta-trefoil, cytokine, polymorphism, secreted
Biological sourceHomo sapiens (human)
Total number of polymer chains1
Total formula weight18159.30
Authors
Lingel, A.,Fairbrother, W. (deposition date: 2009-07-06, release date: 2009-11-17, Last modification date: 2024-05-08)
Primary citationLingel, A.,Weiss, T.M.,Niebuhr, M.,Pan, B.,Appleton, B.A.,Wiesmann, C.,Bazan, J.F.,Fairbrother, W.J.
Structure of IL-33 and its interaction with the ST2 and IL-1RAcP receptors--insight into heterotrimeric IL-1 signaling complexes.
Structure, 17:1398-1410, 2009
Cited by
PubMed Abstract: Members of the interleukin-1 (IL-1) family of cytokines play major roles in host defense and immune system regulation in infectious and inflammatory diseases. IL-1 cytokines trigger a biological response in effector cells by assembling a heterotrimeric signaling complex with two IL-1 receptor chains, a high-affinity primary receptor and a low-affinity coreceptor. To gain insights into the signaling mechanism of the novel IL-1-like cytokine IL-33, we first solved its solution structure and then performed a detailed biochemical and structural characterization of the interaction between IL-33, its primary receptor ST2, and the coreceptor IL-1RAcP. Using nuclear magnetic resonance data, we obtained a model of the IL-33/ST2 complex in solution that is validated by small-angle X-ray scattering (SAXS) data and is similar to the IL-1beta/IL-1R1 complex. We extended our SAXS analysis to the IL-33/ST2/IL-1RAcP and IL-1beta/IL-1R1/IL-1RAcP complexes and propose a general model of the molecular architecture of IL-1 ternary signaling complexes.
PubMed: 19836339
DOI: 10.1016/j.str.2009.08.009
PDB entries with the same primary citation
Experimental method
SOLUTION NMR
Structure validation

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数据于2025-06-18公开中

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